Mutagenetix > Incidental Mutation

Incidental Mutation 'IGL02114:Gm16686'

280295

Institutional Source

Australian Phenomics Network (link to record)

Gene Symbol

Gm16686

Ensembl Gene

ENSMUSG00000085473

Gene Name

predicted gene, 16686

Synonyms

Accession Numbers

Essential gene?

Probably non essential (E-score: 0.071) question?

Stock #

IGL02114

Quality Score

Status

Chromosome

Chromosomal Location

(GRCm39)

Type of Mutation

missense

DNA Base Change (assembly)

A to T at 88673739 bp (GRCm39)

Zygosity

Heterozygous

Amino Acid Change

Leucine to Glutamine at position 30 (L30Q)

Ref Sequence

ENSEMBL: ENSMUSP00000127029 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000094992] [ENSMUST00000141816] [ENSMUST00000191112]

AlphaFold

no structure available at present

Predicted Effect

probably benign
Transcript: ENSMUST00000094992

SMART Domains

Protein: ENSMUSP00000092600
Gene: ENSMUSG00000094618

Domain	Start	End	E-Value	Type
signal peptide	1	21	N/A	INTRINSIC
IFabd	58	170	7.8e-13	SMART

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000097988

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000117750

Predicted Effect

probably null
Transcript: ENSMUST00000141816
AA Change: L30Q

SMART Domains

Protein: ENSMUSP00000127029
Gene: ENSMUSG00000085473
AA Change: L30Q

Domain	Start	End	E-Value	Type
low complexity region	54	71	N/A	INTRINSIC

Predicted Effect

probably null
Transcript: ENSMUST00000191112

SMART Domains

Protein: ENSMUSP00000139768
Gene: ENSMUSG00000100505

Domain	Start	End	E-Value	Type
signal peptide	1	21	N/A	INTRINSIC
IFabd	58	170	1.65e-11	SMART

Coding Region Coverage

Validation Efficiency

Allele List at MGI

Other mutations in this stock

Total: 40 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
1700084J12Rik	C	A	15: 33,405,844 (GRCm39)		probably benign	Het
Akap3	T	C	6: 126,842,959 (GRCm39)	V526A	probably damaging	Het
Ano6	C	A	15: 95,841,341 (GRCm39)	S479R	probably damaging	Het
Aqp8	C	A	7: 123,063,419 (GRCm39)	H90N	probably damaging	Het
Arih1	A	T	9: 59,333,452 (GRCm39)	C229S	probably damaging	Het
Col6a6	C	A	9: 105,644,398 (GRCm39)		probably null	Het
Cp	A	G	3: 20,020,511 (GRCm39)	E168G	probably benign	Het
Creb5	C	T	6: 53,581,443 (GRCm39)		probably benign	Het
Cstdc3	T	A	16: 36,131,617 (GRCm39)	Y42*	probably null	Het
Cyp2c66	C	A	19: 39,159,519 (GRCm39)		probably benign	Het
Dcpp2	C	A	17: 24,119,609 (GRCm39)	A141D	possibly damaging	Het
Dnah5	A	G	15: 28,397,270 (GRCm39)	D3321G	probably damaging	Het
Ecsit	T	C	9: 21,989,440 (GRCm39)		probably benign	Het
Gabra1	T	C	11: 42,026,402 (GRCm39)	I297V	probably damaging	Het
Gja8	T	C	3: 96,827,341 (GRCm39)	K107R	probably benign	Het
Hbp1	T	C	12: 31,980,674 (GRCm39)		probably benign	Het
Inhbc	T	C	10: 127,205,971 (GRCm39)	I99V	probably benign	Het
Kcne3	T	A	7: 99,833,697 (GRCm39)		probably benign	Het
Larp1	T	C	11: 57,947,881 (GRCm39)	Y926H	probably damaging	Het
Lhfpl5	G	T	17: 28,795,149 (GRCm39)	A59S	possibly damaging	Het
Mov10	T	A	3: 104,702,634 (GRCm39)		probably benign	Het
Myl12b	A	T	17: 71,284,164 (GRCm39)	N21K	possibly damaging	Het
Ncoa7	A	T	10: 30,538,360 (GRCm39)	V675E	probably damaging	Het
Nt5c1b	T	C	12: 10,425,444 (GRCm39)	I255T	probably damaging	Het
Numa1	T	A	7: 101,661,083 (GRCm39)		probably benign	Het
Or13c3	T	A	4: 52,856,144 (GRCm39)	Y123F	probably damaging	Het
Otop2	A	T	11: 115,217,806 (GRCm39)	D214V	possibly damaging	Het
Plec	C	A	15: 76,057,748 (GRCm39)	G3928V	probably damaging	Het
Prkcz	T	C	4: 155,356,047 (GRCm39)	E176G	probably damaging	Het
Qdpr	G	A	5: 45,592,018 (GRCm39)	T106I	possibly damaging	Het
R3hdm2	T	G	10: 127,319,978 (GRCm39)	M481R	probably damaging	Het
Setdb2	C	T	14: 59,639,764 (GRCm39)	R709Q	probably damaging	Het
Skic2	C	T	17: 35,060,092 (GRCm39)	V145M	probably damaging	Het
Slx4ip	T	A	2: 136,842,120 (GRCm39)	V15D	probably damaging	Het
Stat4	T	C	1: 52,142,024 (GRCm39)	S624P	probably damaging	Het
Tecpr2	T	A	12: 110,935,321 (GRCm39)	L1380Q	probably damaging	Het
Traf2	T	C	2: 25,415,004 (GRCm39)	I286V	possibly damaging	Het
Vmn2r30	T	C	7: 7,340,408 (GRCm39)	I29V	possibly damaging	Het
Wdr43	A	G	17: 71,959,843 (GRCm39)	Q561R	probably benign	Het
Zfp607b	T	A	7: 27,403,150 (GRCm39)	F535L	probably benign	Het

Other mutations in Gm16686

Allele	Source	Chr	Coord	Type	Predicted Effect
R4293:Gm16686	UTSW	4	88,673,710 (GRCm39)	unclassified	probably benign
R4752:Gm16686	UTSW	4	88,673,725 (GRCm39)	unclassified	probably benign
R5478:Gm16686	UTSW	4	88,673,714 (GRCm39)	unclassified	probably benign
R5485:Gm16686	UTSW	4	88,673,641 (GRCm39)	unclassified	probably benign
R6518:Gm16686	UTSW	4	88,673,725 (GRCm39)	unclassified	probably benign
R7426:Gm16686	UTSW	4	88,673,563 (GRCm39)	missense	unknown
R8711:Gm16686	UTSW	4	88,673,473 (GRCm39)	missense	unknown
R8738:Gm16686	UTSW	4	88,673,775 (GRCm39)	missense	unknown

Posted On

2015-04-16